Holistic Medicine Treatment of Uterine Fibroids-Adults

NCT ID: NCT07219381

Last Updated: 2025-12-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

NA

Total Enrollment

75 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-06-26

Study Completion Date

2029-01-19

Brief Summary

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This clinical trial aims to evaluate the efficacy of holistic medicine treatments for unmarried women ("Bachelorettes") residing on U.S. Tribal Lands or in the State of Alaska who have been clinically diagnosed with uterine fibroids. The study will assess both primary and secondary outcomes, while accounting for socioeconomic and cultural factors that may influence treatment efficacy and data validity. The research acknowledges the unique sociocultural and economic contexts of Tribal communities and aims to contribute to equitable healthcare research practices, with particular attention to urban poverty, unmarried status, and substance-free lifestyle factors.

DECEMBER 9, 2025 SERVICE DELIVERY UPGRADE:

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Detailed Description

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OBJECTIVES:

To evaluate the clinical efficacy of holistic medicine treatments for uterine fibroids among unmarried women on Tribal Lands or in the State of Alaska, with focus on urban and economically disadvantaged populations.

To assess the influence of socioeconomic factors including urban poverty, marital status, and substance-free lifestyle choices on treatment outcomes.

To identify barriers to participation and data validity arising from systemic inequities affecting Tribal communities and urban populations experiencing poverty.

Conditions

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Uterine Fibroids - 1St Diagnosis Uterine Fibroids Affecting Pregnancy Uterine Fibroid Degenerated

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Holistic Medicine, also known as Holistic Education, represents a nonclinical approach to healing, recovery and wellness. It focuses on nurturing the whole person-mind, body, and spirit-to achieve optimal well-being. Other names for this intervention include Nonclinical Variables and Adult Education.

The Patient-Centered Medical Home (PCMH) model plays a crucial role in delivering holistic care. PCMH provides individualized care, patient engagement, and comprehensive care coordination within a single practice. The ultimate goal is to improve quality of life through prevention education, treatment, and rehabilitation programs tailored to individual patient needs.

Holistic Medicine (Holistic Education) emphasizes patient self-help and self-care.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Resource Utilization Group (RUG)

nonclinical variables

Group Type EXPERIMENTAL

Holistic Medicine (HM)

Intervention Type BEHAVIORAL

With informed consent the participant act as a partner to their health and acknowledges responsibility for self-help or self-care directed activities in a non-clinical setting. Transcendence in research involves actively exploring the best possible options or resources for a resolution or self-determination or hypotheses. To reinforce healthy activities, periodic forecast consist of one or more of the following variables: pastoral counseling, lectures, group discussions, sound therapy, team building exercises, faith-based initiatives, outdoor exercise, walking group, support group, supportive care, cooking class, critical thinking questioning and self-assessment tests. Adult content variables are classified under gender-specific care Respite ( i.e. watch party, gaming, music therapy, interactive Spiritual story, clothing model therapy, portable foot spa and portable foot massage) TO (Time-Out).

Interventions

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Holistic Medicine (HM)

With informed consent the participant act as a partner to their health and acknowledges responsibility for self-help or self-care directed activities in a non-clinical setting. Transcendence in research involves actively exploring the best possible options or resources for a resolution or self-determination or hypotheses. To reinforce healthy activities, periodic forecast consist of one or more of the following variables: pastoral counseling, lectures, group discussions, sound therapy, team building exercises, faith-based initiatives, outdoor exercise, walking group, support group, supportive care, cooking class, critical thinking questioning and self-assessment tests. Adult content variables are classified under gender-specific care Respite ( i.e. watch party, gaming, music therapy, interactive Spiritual story, clothing model therapy, portable foot spa and portable foot massage) TO (Time-Out).

Intervention Type BEHAVIORAL

Other Intervention Names

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Holistic Education Transcendence Research Adult Education

Eligibility Criteria

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Inclusion Criteria

* Be a Bachelorette (single, never married, divorced, widowed, or separated) who is age 21-55.
* Have been told by a doctor that you have uterine fibroids (non-cancerous growths in your uterus).
* Live on Tribal Lands or anywhere in the State of Alaska,
* Be willing to try natural, nonclinical holistic treatments alongside regular clinical medical care.
* Acknowledge smoke-free, drug-free, and alcohol-free policy for this clinical trial.
* Must have income or resources for means-tested free program
* Must have access to the internet, own a King James Version Holy Bible and a portable fetal Doppler to listen to and monitor uterine fibroid heart rate in spiritual mysteries.
* Religious or spiritual belief in prayer meditation for faith-based healing.
* Must agree to medical ethical standards in Greek text pertaining to the Hippocratic Oath.
* Due to a new tool in the Toolkit: DOGS HELP TO DETECT COVID-19, a negative COVID-19 test may be required at any time whenever COVID-19 is suspected without remedy.

You May Still Qualify Even If:

* You haven't tried other treatments yet.
* You're currently receiving other fibroid treatments.
* You live in a remote area with limited healthcare access.
* You prefer natural or traditional healing approaches.
* You have concerns about surgery or medications.

* Married relationship status
* Gender conversion
* Repeat Offenders
* No income or resources for means-tested free program.
* Smokers, vapors, alcoholics, drug abusers.
* Non-Believers in Christian religious practices or prayer.
* Immobility
* Diseases without clinical diagnosis, medical treatment, and remedy.
* Uterine Fibroids premature removal by invasive/noninvasive surgery or Birth Control before climacteric.
* Unreported violence or abuse can inadvertently influence the validity of this study.
Minimum Eligible Age

21 Years

Maximum Eligible Age

55 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Virtual Tribunal Monastery

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jones

Role: STUDY_CHAIR

Humanitarian Veterans Association

Locations

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Virtual Tribunal Monastery

Anchorage, Alaska, United States

Site Status

Countries

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United States

Other Identifiers

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RYXWWMJUDPM6-Bachelorettes

Identifier Type: -

Identifier Source: org_study_id